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Items: 1 to 20 of 40

1.

Validation, Identification, and Biological Consequences of the Site-specific O-GlcNAcylation Dynamics of Carbohydrate-responsive Element-binding Protein (ChREBP).

Yang AQ, Li D, Chi L, Ye XS.

Mol Cell Proteomics. 2017 Jul;16(7):1233-1243. doi: 10.1074/mcp.M116.061416. Epub 2017 Apr 27.

PMID:
28450420
2.

MNT and Emerging Concepts of MNT-MYC Antagonism.

Yang G, Hurlin PJ.

Genes (Basel). 2017 Feb 20;8(2). pii: E83. doi: 10.3390/genes8020083.

3.

MondoA coordinately regulates skeletal myocyte lipid homeostasis and insulin signaling.

Ahn B, Soundarapandian MM, Sessions H, Peddibhotla S, Roth GP, Li JL, Sugarman E, Koo A, Malany S, Wang M, Yea K, Brooks J, Leone TC, Han X, Vega RB, Kelly DP.

J Clin Invest. 2016 Sep 1;126(9):3567-79. doi: 10.1172/JCI87382. Epub 2016 Aug 8.

4.

The role of the glucose-sensing transcription factor carbohydrate-responsive element-binding protein pathway in termite queen fertility.

Sillam-Dussès D, Hanus R, Poulsen M, Roy V, Favier M, Vasseur-Cognet M.

Open Biol. 2016 May;6(5). pii: 160080. doi: 10.1098/rsob.160080. Epub 2016 May 18. Erratum in: Open Biol. 2016 Oct;6(10 ):.

5.

The glucose-sensing transcription factor MLX promotes myogenesis via myokine signaling.

Hunt LC, Xu B, Finkelstein D, Fan Y, Carroll PA, Cheng PF, Eisenman RN, Demontis F.

Genes Dev. 2015 Dec 1;29(23):2475-89. doi: 10.1101/gad.267419.115. Epub 2015 Nov 19.

6.

The Regulation of Muscle Structure and Metabolism by Mio/dChREBP in Drosophila.

Polak GL, Pasqualino A, Docherty JE, Beck SJ, DiAngelo JR.

PLoS One. 2015 Aug 25;10(8):e0136504. doi: 10.1371/journal.pone.0136504. eCollection 2015.

7.

Metabolic reprogramming in triple-negative breast cancer through Myc suppression of TXNIP.

Shen L, O'Shea JM, Kaadige MR, Cunha S, Wilde BR, Cohen AL, Welm AL, Ayer DE.

Proc Natl Acad Sci U S A. 2015 Apr 28;112(17):5425-30. doi: 10.1073/pnas.1501555112. Epub 2015 Apr 13.

8.

MondoA-Mlx transcriptional activity is limited by mTOR-MondoA interaction.

Kaadige MR, Yang J, Wilde BR, Ayer DE.

Mol Cell Biol. 2015 Jan;35(1):101-10. doi: 10.1128/MCB.00636-14. Epub 2014 Oct 20.

9.

MondoA deficiency enhances sprint performance in mice.

Imamura M, Chang BH, Kohjima M, Li M, Hwang B, Taegtmeyer H, Harris RA, Chan L.

Biochem J. 2014 Nov 15;464(1):35-48. doi: 10.1042/BJ20140530.

10.

Drosophila Myc: A master regulator of cellular performance.

Grifoni D, Bellosta P.

Biochim Biophys Acta. 2015 May;1849(5):570-81. doi: 10.1016/j.bbagrm.2014.06.021. Epub 2014 Jul 8. Review.

11.

Functional interactions among members of the MAX and MLX transcriptional network during oncogenesis.

Diolaiti D, McFerrin L, Carroll PA, Eisenman RN.

Biochim Biophys Acta. 2015 May;1849(5):484-500. doi: 10.1016/j.bbagrm.2014.05.016. Epub 2014 May 22. Review.

12.

The Caenorhabditis elegans Myc-Mondo/Mad complexes integrate diverse longevity signals.

Johnson DW, Llop JR, Farrell SF, Yuan J, Stolzenburg LR, Samuelson AV.

PLoS Genet. 2014 Apr 3;10(4):e1004278. doi: 10.1371/journal.pgen.1004278. eCollection 2014 Apr.

13.

An overview of MYC and its interactome.

Conacci-Sorrell M, McFerrin L, Eisenman RN.

Cold Spring Harb Perspect Med. 2014 Jan 1;4(1):a014357. doi: 10.1101/cshperspect.a014357. Review. Erratum in: Cold Spring Harb Perspect Med. 2014 Apr;4(4). doi:10.1101/cshperspect.a023325.

14.

Coordination of nutrient availability and utilization by MAX- and MLX-centered transcription networks.

O'Shea JM, Ayer DE.

Cold Spring Harb Perspect Med. 2013 Sep 1;3(9):a014258. doi: 10.1101/cshperspect.a014258. Review.

15.

MondoA senses adenine nucleotides: transcriptional induction of thioredoxin-interacting protein.

Han KS, Ayer DE.

Biochem J. 2013 Jul 15;453(2):209-18. doi: 10.1042/BJ20121126.

16.

dMyc expression in the fat body affects DILP2 release and increases the expression of the fat desaturase Desat1 resulting in organismal growth.

Parisi F, Riccardo S, Zola S, Lora C, Grifoni D, Brown LM, Bellosta P.

Dev Biol. 2013 Jul 1;379(1):64-75. doi: 10.1016/j.ydbio.2013.04.008. Epub 2013 Apr 19.

17.

Mondo/ChREBP-Mlx-regulated transcriptional network is essential for dietary sugar tolerance in Drosophila.

Havula E, Teesalu M, Hyötyläinen T, Seppälä H, Hasygar K, Auvinen P, Orešič M, Sandmann T, Hietakangas V.

PLoS Genet. 2013 Apr;9(4):e1003438. doi: 10.1371/journal.pgen.1003438. Epub 2013 Apr 4.

18.

Glucose induces protein targeting to glycogen in hepatocytes by fructose 2,6-bisphosphate-mediated recruitment of MondoA to the promoter.

Petrie JL, Al-Oanzi ZH, Arden C, Tudhope SJ, Mann J, Kieswich J, Yaqoob MM, Towle HC, Agius L.

Mol Cell Biol. 2013 Feb;33(4):725-38. doi: 10.1128/MCB.01576-12. Epub 2012 Dec 3.

19.

Adaptive metabolic response to 4 weeks of sugar-sweetened beverage consumption in healthy, lightly active individuals and chronic high glucose availability in primary human myotubes.

Sartor F, Jackson MJ, Squillace C, Shepherd A, Moore JP, Ayer DE, Kubis HP.

Eur J Nutr. 2013 Apr;52(3):937-48. doi: 10.1007/s00394-012-0401-x. Epub 2012 Jun 26.

20.

A novel N-terminal domain may dictate the glucose response of Mondo proteins.

McFerrin LG, Atchley WR.

PLoS One. 2012;7(4):e34803. doi: 10.1371/journal.pone.0034803. Epub 2012 Apr 10.

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